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Ethyl 3-(2',4'-dimethoxyphenyl)but-2-enoate is an organic compound with the chemical formula C13H16O4. It is a derivative of cinnamic acid, featuring a phenyl ring with two methoxy groups at the 2' and 4' positions, and a but-2-enoate group attached to the 3-position. ethyl 3-(2',4'-dimethoxyphenyl)but-2-enoate is characterized by its aromatic scent and is often used in the fragrance and flavor industries due to its pleasant odor. It can be synthesized through various chemical reactions, such as the esterification of 3-(2',4'-dimethoxyphenyl)but-2-enoic acid with ethanol. Ethyl 3-(2',4'-dimethoxyphenyl)but-2-enoate is also known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its chemical structure and properties make it a versatile compound in the realm of organic chemistry.

7760-63-6

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7760-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7760-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,6 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7760-63:
(6*7)+(5*7)+(4*6)+(3*0)+(2*6)+(1*3)=116
116 % 10 = 6
So 7760-63-6 is a valid CAS Registry Number.

7760-63-6Downstream Products

7760-63-6Relevant academic research and scientific papers

Environmentally friendly synthesis of coumarin derivatives employing heterogeneous catalysis

Gunnewegh,Hoefnagel,Downing,Van Bekkum

, p. 226 - 230 (2007/10/03)

Zeolite H-BEA and other solid acids have been shown to be effective catalysts for the production of coumarin derivatives from activated phenols and acids or esters possessing an additional alkylation function, or β-keto esters (Pechmann reaction). These heterogeneous catalysts eliminate the production of acidic waste streams associated with conventional (Lewis) acid catalysts. Zeolite H-BEA proved to be the preferred catalyst.

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